85370069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110549976-C-T

85370073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110549980-A-G

http://identifiers.org/hco/13/GRCh38#85370079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110549986-A-C

85370137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550046-A-G

85370424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550302-G-T

85370450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550327-G-A

85370480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550354-C-T

85370569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550439-A-G

85370588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550460-C-T

http://identifiers.org/hco/13/GRCh38#85370623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110550488-C-A

85370623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550488-C-T

85370735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550608-G-C

85370735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550608-G-T

85370901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550773-T-C

85370941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550790-T-G

85370986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550831-A-G

85371111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550955-G-A

85371111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110550955-G-T

http://identifiers.org/hco/13/GRCh38#85375228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110551127-C-A

85375300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551200-G-C

85375528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551393-A-G

85375542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551407-G-C

85375600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551474-C-G

85375654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551529-C-G

85375725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551596-G-C

85375725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551596-G-T

85375736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551603-C-T

85375790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551660-T-C

85375825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551693-A-G

85375916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551775-T-C

85376116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551985-G-A

85376116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551985-G-T

85376121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110551990-G-A

85376344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552154-T-A

85376389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552204-A-G

85376421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552242-C-G

85376604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552403-T-C

85376833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552598-G-C

85376918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110552670-C-T

85378350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558361-T-C

85378379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558390-C-T

85378380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558391-A-T

85378520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558519-T-C

85378826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558830-C-G

85378844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558848-C-T

85378862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110558866-C-T

85378998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110559001-C-G

85378998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110559001-C-T

85379053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110559063-C-T

85382792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563236-G-T

85382799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563243-G-T

85382847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563293-T-G

85382895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563338-C-T

85382896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563339-C-G

85382896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563339-C-T

85383163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563564-A-T

85383215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563616-G-C

85383339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563740-G-A

85383339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110563740-G-T

85383623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110564008-C-T

85383728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110564104-G-T

85383754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110564142-C-T

85385611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110568705-A-G

85385805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110568874-C-T

85385808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110568877-G-T

85386338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110569401-G-A

85386479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110569544-A-G

85386565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110569621-T-C

85386685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110569753-T-C

85387054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570107-A-G

85387115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570165-C-T

85387129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570180-G-A

85387145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570196-G-A

85387218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570269-G-T

85387521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570492-A-G

85387534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110570501-T-G

85405150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110578979-G-C

85408700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110580670-A-G

85410758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588255-T-C

85410840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588310-G-A

85410857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588326-T-C

85410865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588336-C-T

85410882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588354-C-T

85410995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588452-T-A

85411058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588519-C-G

http://identifiers.org/hco/13/GRCh38#85411246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110588697-C-A

85411256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588707-A-G

85411388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588839-G-A

85411482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588931-C-T

85411578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589019-C-T

85411586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589027-C-T

85411776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110589181-A-G

85411790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110589186-A-G

85411828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110589224-A-G

85412072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110591163-T-A

85412772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110591801-G-A

85412792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110591821-G-A

85413223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592196-A-G

85413235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592208-A-G

http://identifiers.org/hco/13/GRCh38#85413405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110592411-A-C

85413667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110593006-G-A

85413848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110593199-A-G

85414802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110604925-A-G

http://identifiers.org/hco/13/GRCh38#85414862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110604977-C-A

85414862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110604977-C-T

85414981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605084-T-G

85414996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605101-C-G

85415020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605122-C-T

85415184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605291-A-G

85415184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605291-A-T

85415225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605342-A-G

85415394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605549-G-T

85415539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605688-T-G

85415600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605760-T-C

85415624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110605791-C-T

85416718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110611389-A-G

85416841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110611481-G-A

85416847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110611486-G-T

85419651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614355-A-G

85419767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614466-C-G

85419788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614486-G-A

85419788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614486-G-C

85419907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614628-A-G

85419947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614668-T-C

85419957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110614678-T-C

85420524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110615182-T-C

85420796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110615430-T-A

85421014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110615711-G-A

85421063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110615763-T-C

85421356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110616053-C-T

http://identifiers.org/hco/13/GRCh38#85421528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110616206-A-C

85421528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110616206-A-G

85422405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110616890-G-A

85422456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110616943-T-A

85422463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110616950-A-T

85422558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110617025-T-C

85422814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110617269-A-T

85425976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110619904-T-C

85426206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110620137-A-T

85426420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110620317-G-A

85426559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110620451-G-T

http://identifiers.org/hco/13/GRCh38#85429905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110625434-A-C

85429905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625434-A-G

85429983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625515-C-T

85430100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625609-T-C

85430193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625677-A-G

http://identifiers.org/hco/13/GRCh38#85430196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110625680-A-C

85430196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625680-A-G

85430216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625699-C-G

85430268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625748-A-G

85430428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625912-G-A

85430429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625913-G-A

85430429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625913-G-T

85430481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110625967-G-A

http://identifiers.org/hco/13/GRCh38#85430511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110625997-C-A

85430611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110626105-T-C

85430658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110626152-C-G

85432568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110626506-T-G

85432963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110626922-C-T

85433076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627037-C-T

85433243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627176-A-G

85433248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627181-T-C

85433281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627214-C-T

85433290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627223-G-A

85433327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627264-G-A

85433363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627308-T-C

85433419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627429-T-C

85433488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110627498-T-C

85434392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110628804-A-G

http://identifiers.org/hco/13/GRCh38#85434406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110628818-A-C

85434441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110628856-A-G

85434509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110628911-A-G

85434681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110629034-G-C

85434681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110629034-G-T

http://identifiers.org/hco/13/GRCh38#85434737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110629100-C-A

85435052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110629404-A-G

85435083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110629434-C-G

85435083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110629434-C-T

85435758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110631455-G-C

85435848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110631543-T-C

85436461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632118-G-A

85436532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632195-A-T

85436764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632420-C-T

85436776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632433-G-A

85436902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632562-T-C

85436946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632606-T-C

85436955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632614-G-A

85437009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632671-C-T

85437038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632699-T-C

85437173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110632811-A-G

85437766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110633274-A-G

85437777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110633277-G-A

85437794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110633294-T-C

85437891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110633384-G-A

85441262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110638452-G-A

http://identifiers.org/hco/13/GRCh38#85441300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110638488-A-C

85441315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110638503-A-G

85441399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110638587-T-C

85441486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110638671-C-G

85441496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110638681-T-A

http://identifiers.org/hco/13/GRCh38#85441947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110638838-A-C

85442230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639089-G-A

85442302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639165-A-G

85442354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639223-G-A

85442402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639270-G-A

85442402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639270-G-C

85442402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639270-G-T

85442472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639340-C-T

85442478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639346-T-C

85442500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639368-G-A

85442640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639485-C-T

http://identifiers.org/hco/13/GRCh38#85442748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110639570-A-C

85442748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639570-A-T

85442855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639682-G-C

http://identifiers.org/hco/13/GRCh38#85442871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110639698-A-C

85442871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639698-A-T

85442924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110639747-A-T

85443093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110643552-A-G

http://identifiers.org/hco/13/GRCh38#85443329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110647292-C-A

85443446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110647403-A-G

85443446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110647403-A-T

http://identifiers.org/hco/13/GRCh38#85443451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110647408-C-A

85443451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110647408-C-T

http://identifiers.org/hco/13/GRCh38#85443542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110647493-A-C

85446045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110655841-A-G

85446108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110655921-G-T

85446201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656009-A-G

85446257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656063-G-A

85446435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656249-T-C

85446453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656267-G-T

http://identifiers.org/hco/13/GRCh38#85446499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110656311-A-C

85446513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656325-G-T

85446730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110656517-G-T

85447230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658227-A-G

85447230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658227-A-T

85447390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658372-T-A

85447457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658436-T-C

85447590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658573-A-G

85447636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658619-G-T

85447645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658630-G-T

85447730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110658712-T-C

85448249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660315-T-C

http://identifiers.org/hco/13/GRCh38#85448386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110660430-A-C

85448490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660534-G-A

85448491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660535-T-C

85448543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660577-G-A

85448553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660587-T-G

http://identifiers.org/hco/13/GRCh38#85448656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110660689-A-C

85448682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660715-G-A

85448828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660862-A-G

85448939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110660972-T-C

85449635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110665795-C-G

85460608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666612-T-A

85460648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666658-T-A

85460700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666708-G-A

85460700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666708-G-T

85460830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666833-C-T

85460845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666842-G-A

85460947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110666927-T-A

85461079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667050-C-T

85461203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667151-A-G

85461211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667158-G-A

85461341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667277-A-T

85461346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667282-A-T

85461442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667389-G-A

http://identifiers.org/hco/13/GRCh38#85461788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110667726-C-A

85461804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667742-G-A

85461876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667814-T-A

85461878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110667816-C-T

85467338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670151-C-T

85467359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670178-G-A

85467372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670190-T-C

85467472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670254-T-A

85467476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670258-C-T

85467554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670335-G-A

85467580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670361-G-A

85467616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670397-A-G

85467716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670491-A-G

85467849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670613-C-T

85468118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110670860-A-G

85469389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110672626-T-C

http://identifiers.org/hco/13/GRCh38#85469440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110672673-C-A

85469440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110672673-C-T

http://identifiers.org/hco/13/GRCh38#85469460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110672685-C-A

85469477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110672702-A-T

85469621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110672833-T-C

85469677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110672889-G-T

85469854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110673061-C-G

http://identifiers.org/hco/13/GRCh38#85470005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110673205-C-A

85470129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676245-C-T

http://identifiers.org/hco/13/GRCh38#85470168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110676285-C-A

85470221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676338-A-T

85470225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676342-A-T

85470370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676450-C-T

85470603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676717-A-G

85470623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676737-G-C

85470694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676816-T-A

85470701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110676821-T-C

http://identifiers.org/hco/13/GRCh38#85470732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110676851-C-A

85470931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110677018-C-T

http://identifiers.org/hco/13/GRCh38#85471052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110677136-C-A

85471059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110677143-T-A

http://identifiers.org/hco/13/GRCh38#85471306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110677351-A-C

85471382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110677417-T-C

85471435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110677471-A-G

http://identifiers.org/hco/13/GRCh38#85471565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110677595-C-A

85471623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110678616-G-T

85471673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110678664-A-G

85471744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110678741-G-T

http://identifiers.org/hco/13/GRCh38#85471827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110678818-C-A

85471888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110678879-T-A

85472237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679203-T-C

85472338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679287-A-G

85472421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679369-G-T

85472426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679374-C-T

85472452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679408-T-G

85472478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679457-A-G

85472547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679525-T-A

85472630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679603-T-C

85472631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679604-G-T

85472653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679626-T-A

85473210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679900-G-C

85473225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110679913-C-T

85473475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110680171-T-G

85473562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110680253-A-G

85473763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681337-G-C

85473763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681337-G-T

85473784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681358-G-A

85473906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681445-T-C

85474023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681562-C-T

85474035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681574-G-T

85474036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681575-A-G

85474213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681747-A-G

85474222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681756-G-A

85474459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110681975-G-C

85474519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682022-G-A

85474519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682022-G-T

85474520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682023-T-C

85474583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682089-T-C

85476894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682886-G-A

85477008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682987-A-G

85477008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110682987-A-T

http://identifiers.org/hco/13/GRCh38#85477138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110683102-C-A

85477138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683102-C-T

http://identifiers.org/hco/13/GRCh38#85477211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110683175-A-C

85477212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683176-A-G

85477357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683321-C-G

85477407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683373-C-G

85477487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683477-G-A

85477523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683533-T-G

85477557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683567-T-G

85477804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683799-A-G

85477815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683811-T-A

85477920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110683908-G-T

85478150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684235-A-G

85478152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684237-T-C

85478192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684279-G-C

85478271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684418-G-A

85478346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684490-C-T

85478377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684521-G-A

http://identifiers.org/hco/13/GRCh38#85478386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110684530-C-A

85478432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684570-T-G

85478479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684595-G-C

85478490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684606-C-T

85478513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684622-T-G

85478548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684655-G-A

85478614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684721-A-G

85478615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684722-C-G

85478657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110684748-A-T

http://identifiers.org/hco/13/GRCh38#85478673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110684764-C-A

85478883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685126-T-A

85478891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685134-T-A

85478927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685169-A-G

85478927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685169-A-T

85479020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685261-T-C

85479026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685267-A-G

85479213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685460-A-T

85479223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685470-C-T

85479422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685666-T-C

85479452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685696-C-T

85479560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685806-C-T

85479696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685949-A-G

85479704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685957-C-T

85479730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685990-A-G

85479733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110685993-T-C

http://identifiers.org/hco/13/GRCh38#85479755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110686014-A-C

85479784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110686045-G-C

85479908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110686155-T-G

85488062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110689842-G-A

85488084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110689867-A-G

85488217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110689979-A-G

85488226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110689989-G-C

85488457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110690205-T-G

85488547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110690296-A-G

85488547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110690296-A-T

85488667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110690413-G-T

85488762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110690495-A-G

http://identifiers.org/hco/13/GRCh38#85489233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110692414-C-A

85489291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692471-T-C

85489410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692590-C-T

http://identifiers.org/hco/13/GRCh38#85489520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110692713-A-C

85489586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692781-T-A

85489624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692816-G-C

85489624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692816-G-T

85489658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692839-T-C

http://identifiers.org/hco/13/GRCh38#85489664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110692845-C-A

85489787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692976-C-G

85489808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692997-G-A

85489833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693022-G-A

85489876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693065-T-A

http://identifiers.org/hco/13/GRCh38#85489904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110693093-A-C

85489904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693093-A-G

85489920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693109-A-G

http://identifiers.org/hco/13/GRCh38#85489934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110693123-A-C

85490000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693177-G-C

85490173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693325-G-T

85503753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110696681-G-A

85503829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110696759-G-T

85503978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110696890-G-T

http://identifiers.org/hco/13/GRCh38#85504355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110697271-C-A

85504356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697272-A-G

85504435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697333-G-T

85513466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699615-T-C

85513583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699716-A-G

85513682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699813-G-A

85513694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699825-C-G

85513714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699845-T-C

85513846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699965-T-G

85513865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110699983-T-G

85513905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700015-T-C

http://identifiers.org/hco/13/GRCh38#85513937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110700043-A-C

85514004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700113-A-G

85514004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700113-A-T

85514062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700167-A-G

85514115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700221-T-C

85514135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700241-T-A

85514292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700369-G-T

85514315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700391-T-G

85514348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700429-C-T

85514437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700521-G-A

85514509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700586-C-T

85514530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700607-G-C

85514601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700712-C-T

85514695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110700802-A-G

85520407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110704933-A-G

85520583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705135-G-C

85520583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705135-G-T

85520765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705294-T-A

http://identifiers.org/hco/13/GRCh38#85520834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110705366-A-C

http://identifiers.org/hco/13/GRCh38#85521247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110705809-C-A

85521272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705833-A-G

85521341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705932-T-C

85521378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110705974-T-C

85521614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110706366-A-G

85521978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110706733-G-T

85522018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110706773-G-C

85522215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110706964-T-C

85527023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708334-A-G

http://identifiers.org/hco/13/GRCh38#85527292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110708621-C-A

85527515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708848-G-A

85527575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708910-A-G

85527608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708941-A-G

85527633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708967-T-A

85527717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709047-A-G

85527765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709094-G-C

85527820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709149-T-A

85527837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709165-G-A

85527837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709165-G-C

85528444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110709693-A-G

85528593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110709826-A-G

http://identifiers.org/hco/13/GRCh38#85528783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#110709973-C-A

85528783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110709973-C-T

85528891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710078-G-A

85529076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710256-A-G

85529100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110710280-A-G

85529242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710422-T-G

85529252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710432-T-G

http://identifiers.org/hco/13/GRCh38#85529364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110710547-C-A

85529520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710696-T-A

http://identifiers.org/hco/13/GRCh38#85529681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110710882-A-C

85529698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710899-A-G

85529808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711010-G-A

85529928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711139-G-T

85529980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711187-T-C

85529992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711199-C-T

85530034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711241-G-A

85530211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711413-G-A

85530242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711443-T-G

85530249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711450-T-A

85530322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711503-T-G

85530340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711521-C-G

85530340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711521-C-T

85530379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711551-G-A

85530613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711648-G-T

85530696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711699-T-C

85530840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711845-T-G

85530883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711860-G-A

85530889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711868-A-G

85530897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711876-T-G

85530898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711880-A-G

85530945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711923-C-T

85530984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711961-C-T

85531987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110713104-T-C

85532377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110713481-G-A

85532968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110714788-G-T

http://identifiers.org/hco/13/GRCh38#85532990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110714810-C-A

85533128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: non coding transcript exon variant
orthologous variants: 110714962-C-T

http://identifiers.org/hco/13/GRCh38#85533231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110715061-A-C

85533325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110715168-C-T

85533378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110715206-T-C

85533446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110715271-C-G

85533731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110715532-T-G

85533825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110715618-A-G

http://identifiers.org/hco/13/GRCh38#85535350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110721202-C-A

85535355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721208-G-A

85535809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721686-G-A

85535884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721764-C-G

85535926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721807-T-C

85536045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721915-G-A

85536059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110721929-A-G

85537392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110722289-T-C

http://identifiers.org/hco/13/GRCh38#85537602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110722513-C-A

85537602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110722513-C-T

http://identifiers.org/hco/13/GRCh38#85537739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110722629-C-A

85537767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110722657-C-T

85537902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110722792-G-C

85538056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110722913-G-C

85538169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723032-A-G

85538513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723377-G-T

85538525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723389-T-C

85538572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723439-C-T

http://identifiers.org/hco/13/GRCh38#85538618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110723484-A-C

85541701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723845-A-G

85541703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723847-A-G

85541752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723894-G-T

85541789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723931-A-T

85541893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110724029-T-C

85541987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110724109-T-C

http://identifiers.org/hco/13/GRCh38#85542378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110724454-C-A

85542430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110724506-T-C

http://identifiers.org/hco/13/GRCh38#85542490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110724534-A-C

http://identifiers.org/hco/13/GRCh38#85542652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#110724678-A-C

85542777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110724784-G-A

85542777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42669
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110724784-G-C